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Mitogenome Announcement

Characterization and phylogenetic analysis of the complete mitochondrial genome of Actinopyga lecanora (Jaeger, 1833) (Holothuriida: Holothuriidae)

, , , , &
Pages 2801-2802 | Received 07 Jun 2021, Accepted 15 Aug 2021, Published online: 31 Aug 2021

Abstract

The white-bottomed sea cucumber, Actinopyga lecanora, is a valuable inshore fisheries resource which is famous for its high nutrition and pharmacological compounds. However, due to morphological plasticity and limited molecular phylogenetic studies, the taxonomic histories in the genus Actinopyga have not been completely resolved yet. Moreover, there remains a complex of cryptic species within Actinopyga, many of which are incorrectly assigned within the family Holothuriidae. In this study, we report the complete mitochondrial genome of A. lecanora. The mitogenome has 15,568 base pairs (63.40% A + T content) and is made up of a total of 37 genes (13 protein-coding, 22 transfer RNAs and 2 ribosomal RNAs), plus a putative control region. This study offers useful mitogenome data for future phylogenetic and taxonomic classification of Holothuriidae.

Sea cucumbers (Holothuroidea), commonly known as holothuroids, are a species-rich group of relatively large benthic invertebrates which only inhabit in marine environments (Miller et al. Citation2017). Many sea cucumber species play an important role in marine benthic ecosystem due to their huge abundance in local benthic community (Uthicke Citation2001). Moreover, holothuroids are important coastal fisheries resources, many of which have highly commercial value in the Southeast Asian market especially in China (Anderson et al. Citation2011). Actinopyga lecanora is a common edible sea cucumber widely distributed throughout the tropical Indo-west Pacific region and has been known as functional food for its relatively high protein and anti-oxidative component (Ghanbari et al. Citation2015). Despite its abundance and economically importance, many sea cucumbers in the genus Actinopyga are being commercialized without clearly taxonomic identification (Ahmed Citation2016) and the mitogenomes of all species in the genus Actinopyga have yet to be sequenced. Mitogenome sequences have proven to be excellent molecular resources for analyzing evolutionary and phylogenetic relationship (Madduppa et al. Citation2017). Here, we report the complete mitochondrial genome of A. lecanora, which will afford useful molecular data for taxonomic and phylogenetic analyses in sea cucumbers.

One individual sample of A. lecanora was collected from the HaiNan province, China (LingShui, 18.384207 N, 109.981511 E) by local diving fishermen. And the whole body specimen (#GH0078) was deposited at Marine biological Museum, Guangxi Institute of Oceanology, Beihai, China (http://www.gxas.cn/kypt/kxpj/kpcg, Shengping Zhong, [email protected]). The total genomic DNA was extracted from the muscle of the specimen using an SQ Tissue DNA Kit (OMEGA, Guangzhou, China) following the manufacturer’s protocol. DNA libraries (350 bp insert) were constructed with the TruSeq NanoTM kit (Illumina, San Diego, CA) and were sequenced (2 × 150 bp paired-end) using HiSeq platform at BGI Company, China. Mitogenome assembly was performed with MITObim (Hahn et al. Citation2013). The complete mitogenome sequence of A. echinites (GenBank accession number: MN793975) (Zhong et al. Citation2020) was chosen as the initial reference sequence for MITObim assembly. Gene annotation was performed by MITOS (Bernt et al. Citation2013).

The complete mitogenome of A. lecanora (GenBank accession number: MW248463) is 15,568 bp in length and it contains a conserved set of 13 protein-coding genes (PCGs), 2 ribosomal RNA genes, 22 transfer RNA genes, and a putative control region. A total of 37 genes were annotated and 227 nucleotides were identified as putative control region. The overall base composition of the mitogenome is estimated to be A 34.64%, T 28.76%, C 21.47% and G 15.13%, with a high A + T content of 63.40%, which is similar, but slight higher than A. echinites (62.94%) (Zhong et al. Citation2020). The phylogenetic analysis inferred from the concatenated nucleotides sequences of 13 PCGs suggests that Actinopyga and Holothuria holothuroids have closely relationship in family Holothuriidae (), which is consistent with the phylogenetic analyses of holothuroids from Indonesia using mitochondrial Cytochrome c oxidase 1 (COI) sequences (Madduppa et al. Citation2017). The mitogenome of A. lecanora identified in this study exhibited 99.52% identity to the “hui” strain (GenBank accession number: MW218894) indicates that A. lecanora have very closely genetic relationship between these strains. These findings will be helpful for better resolving its taxonomic controversy and future conservation.

Figure 1. Phylogenetic tree of 15 species in echinoderms. The complete mitogenomes were downloaded from GenBank and the phylogenic tree based on the concatenated nucleotide sequences of 13 mitochondrial PCGs was constructed by maximum-likelihood method via PhyML online server (http://www.atgc-montpellier.fr/phyml/), using GTR substitution model with 100 bootstrap replicates. The bootstrap values are indicated at each branch nodes, echinoids (Lytechinus variegatus) were rooted to be outgroup species.

Figure 1. Phylogenetic tree of 15 species in echinoderms. The complete mitogenomes were downloaded from GenBank and the phylogenic tree based on the concatenated nucleotide sequences of 13 mitochondrial PCGs was constructed by maximum-likelihood method via PhyML online server (http://www.atgc-montpellier.fr/phyml/), using GTR substitution model with 100 bootstrap replicates. The bootstrap values are indicated at each branch nodes, echinoids (Lytechinus variegatus) were rooted to be outgroup species.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

The genome sequence data that support the findings of this study are openly available in GenBank of NCBI at (https://www.ncbi.nlm.nih.gov/) under the accession no. MW248463. The associated BioProject, SRA, and Bio-Sample numbers are PRJNA734962, SRR14725728, and SAMN19551203, respectively.

Additional information

Funding

This work was financially supported by Scientific Research and Technology Development Program of Guangxi [Grant No. AB16380105], Development Program of High-level Talent Team under Qihuang Project of Guangxi University of Chinese Medicine [Grant No. 2021004], the Team Research Funds for Institute of marine drugs Guangxi University of Chinese Medicine [Grant No. 2018ZD005-A10, 2018ZD005-A20], the National Modern Agricultural Industry Technology System Guangxi Innovation Team [Grant No. nycytxgxcxtd-14-06], Guangxi Science Foundation for Youths [Grant No. 2020GXNSFBA297126], and PhD research startup foundation of Guangxi University of Chinese Medicine [Grant No. 2019BS018].

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